A Patient-Centric Approach To eConsent

A recent webinar orchestrated by Signant brought together experts to engage in a comprehensive dialogue concerning contemporary themes surrounding informed electronic consent within clinical trials. The esteemed panelists highlighted prevalent obstacles, ranging from the limitations of traditional paper-based consent procedures to the profound influence of intricate study designs and operational frameworks.

In addition, speakers also examined two authentic case studies, showcasing how innovative electronic consent solutions centered around patients' needs were able to effectively alleviate challenges for both patients and research sites, offering a myriad of advantages.

Delve into the complete recording below, and don't hesitate to reach out if you have inquiries, seek to connect with our proficient eConsent specialists, or desire additional information.